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Mutant Information

Mutant NameFN4492-S [Download]
GenerationM2
Genus SpeciesOryza Sativa
CultivarKitaake
Alignment File (BAM File)Download FN4492-S Alignment File
Seed AvailabilityYes [Order Seeds]
Mapping
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Variant Information

Single base substitutions: 36
Variant Type Chromosome Position Change Genotype Effect Gene Affected
SBSChr118192317C-AHOMOINTRON
SBSChr118845021C-THOMOINTERGENIC
SBSChr138860088G-THETNON_SYNONYMOUS_CODINGLOC_Os01g66910
SBSChr18224765T-CHETINTERGENIC
SBSChr19414716A-THETNON_SYNONYMOUS_CODINGLOC_Os01g16580
SBSChr10257609C-THETINTERGENIC
SBSChr1112727519G-THETINTRON
SBSChr1113131038T-GHETINTERGENIC
SBSChr118152456G-AHETINTRON
SBSChr1214259175C-AHOMONON_SYNONYMOUS_CODINGLOC_Os12g24870
SBSChr121616012A-THETINTRON
SBSChr128980445C-THOMOINTERGENIC
SBSChr2336414A-GHOMOINTERGENIC
SBSChr2837741T-AHOMOINTERGENIC
SBSChr321570120A-GHETNON_SYNONYMOUS_CODINGLOC_Os03g38840
SBSChr321830678C-THETINTRON
SBSChr325837312T-CHETINTERGENIC
SBSChr326103093G-AHETNON_SYNONYMOUS_CODINGLOC_Os03g46170
SBSChr329154654C-THETINTERGENIC
SBSChr32922510C-THETINTRON
SBSChr331571915G-AHETINTERGENIC
SBSChr429815324G-AHETINTRON
SBSChr515218839C-THETINTRON
SBSChr515218843G-THETINTRON
SBSChr527979829T-GHETNON_SYNONYMOUS_CODINGLOC_Os05g48820
SBSChr529903555G-AHETINTRON
SBSChr55170589A-THETINTERGENIC
SBSChr620188829T-CHETINTERGENIC
SBSChr620936045A-GHETINTERGENIC
SBSChr62383059G-AHETINTERGENIC
SBSChr718385200T-CHOMOSYNONYMOUS_CODING
SBSChr7184007G-AHETINTERGENIC
SBSChr720689103A-GHETSPLICE_SITE_REGION
SBSChr819039592A-THOMOINTERGENIC
SBSChr912398363T-CHOMOUTR_5_PRIME
SBSChr92307505A-GHOMOINTERGENIC

Deletions: 25
Variant Type Chromosome Start End Size (bp) Number of Genes
DeletionChr21111801111811
DeletionChr737053937054910
DeletionChr117381137381229
DeletionChr5143176014317611
DeletionChr9205521820552191
DeletionChr3603721260372186
DeletionChr27367001738000013000
DeletionChr7760132976013301
DeletionChr11794768179476887
DeletionChr7972731797273192
DeletionChr911273397112734036
DeletionChr411889546118895471
DeletionChr9140053651400537914
DeletionChr1114542477145424781
DeletionChr320230098202300991
DeletionChr421221994212219951
DeletionChr322540594225405951
DeletionChr522790489227904901LOC_Os05g38850
DeletionChr12230908992309091920
DeletionChr723871034238710417
DeletionChr1127170986271709871
DeletionChr827871057278710581
DeletionChr130349325303493261
DeletionChr432893831328938321
DeletionChr434462528344625291

Insertions: 11
Variant Type Chromosome Start End Size (bp) Number of Genes
InsertionChr142275968422759681
InsertionChr1014091886140918861
InsertionChr1120665326206653261
InsertionChr1125200701252007011
InsertionChr118578385857840622
InsertionChr12423383342338342
InsertionChr12972102697210261
InsertionChr2150481015048101
InsertionChr223341540233415401
InsertionChr316145258161452592
InsertionChr513597921135979211

Inversions: 3
Variant Type Chromosome Position 1 Position 2 Number of Genes
InversionChr880155958015809
InversionChr91801434818014530
InversionChr32756436327564475

Translocations: 2
Variant Type Chromosome Position 1 Chromosome Position 2 Number of Genes
TranslocationChr89744461Chr316641765LOC_Os03g17540
TranslocationChr628880844Chr27385049